EP0820348A1 - Testkarte für analysen - Google Patents
Testkarte für analysenInfo
- Publication number
- EP0820348A1 EP0820348A1 EP97901736A EP97901736A EP0820348A1 EP 0820348 A1 EP0820348 A1 EP 0820348A1 EP 97901736 A EP97901736 A EP 97901736A EP 97901736 A EP97901736 A EP 97901736A EP 0820348 A1 EP0820348 A1 EP 0820348A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- chambers
- partition
- card
- card according
- cavities
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
- Y10T436/2575—Volumetric liquid transfer
Definitions
- the present invention relates to the processing of an analysis card.
- analysis is meant any process or process making it possible to identify, separate, isolate, determine, detect, or quantify, a material, a product, a substance, or a compound, designated under the generic expression of “analyte ", from a sample or sample to be analyzed, previously diluted or not with any suitable medium, for example a solvent.
- the analyte sought may be of a chemical, biochemical or even biological nature, for example in the latter case an antigen or an antibody.
- analysis card any device, module, or system, arranged internally to carry out the various processes or reactions necessary for the identification, separation, detection or quantification of the analyte, by means of different processing, in particular within said card, or manipulation of the analysis card, for example automatically.
- Such an analysis card well known to those skilled in the art, constitutes a closed assembly vis-à-vis the outside or its immediate environment, with the exception of course of any passages or equivalent means, allowing in particular and initially to introduce the sample or sample to be analyzed.
- Such an analysis card contains the reagent (s), physico-chemical, chemical, biochemical, or biological, distributed and maintained in the card, according to the path of the sample to be analyzed, and the reaction processes or reactions to be carried out to accomplish analysis.
- An analysis card as envisaged by the present invention generally constituting a device or assembly for single use, that is to say discarded or destroyed after its use, comprises or integrates within it a plurality of chambers, arranged 97/28899 PCMB97 / 00112
- analysis cards in series and / or in parallel, one of which, for example the last, is in particular an optical measurement chamber.
- These analysis cards can be produced or produced by any suitable technique, for example in one or more parts assembled (for example welding) together, produced for example by molding one or more identical or different plastics.
- chamber is meant in the claims and description any enclosure, or passage, ensuring the reception and / or circulation of any liquid, fluid, or gas present in the analysis card.
- the present invention relates to a particular analysis card, allowing an operation of connecting at least two chambers, formed in an analysis card, and initially isolated from one another, this operation being carried out remotely and without mechanical action or contact with the analysis card.
- the present invention lies in the cooperation of two essential means, namely, on the one hand, a light beam, in particular coherent, having at least a predetermined wavelength ⁇ , and a predetermined power P, obtained from a light source, in particular a laser, and on the other hand a structure or arrangement of an analysis card, in which are formed at least two chambers isolated from one another, and from the 'exterior; but this structure is specifically adapted to the implementation of this light beam, to establish at least one passage between at least two chambers of said card.
- the two chambers are separated from each other by a partition, perforable, disposed within the card, of absorbent material, in particular plastic, absorbing the light energy of the light beam above, to transform it into thermal energy capable of eliminating at least locally said material; and two cavities are provided on either side of the partition, and are in communication with or included in the two chambers respectively; and a window made of a transparent material at least for the wavelength ⁇ is arranged opposite said partition, and delimits with the latter one of said cavities, called the incidence of a light ray.
- An analysis card in accordance with the present invention makes it possible to implement the following method, and more particularly the following steps, cooperating with each other:
- the light source is controlled or controlled, so that the thermal energy dissipated within the perforable partition does not exceed that necessary for the local elimination of the absorbent material, for example by fusion, vaporization, or sublimation, according to a perforating hole right through this partition, of limited or controlled radial extension.
- the light beam used according to the invention can be convergent, parallel, or divergent, the essential condition being the power density of the light ray striking the perforable partition.
- suitable guiding means can be provided before and / or after the beam, to satisfy the essential condition mentioned above.
- US-C-5 411 065 it has already been proposed to use a laser light beam to remotely perforate a wall.
- the method according to the present invention therefore allows manipulation of the analysis card, in particular by automatic means, leading, in relation to the light beam, in particular laser, to the perforation of any partition, disposed within said card, and this while preserving the rest or the integrity of the latter.
- Such a method therefore appears to be particularly suitable for today's analysis apparatus, working for a large part, if not entirely, automatically.
- FIG. 1 shows, schematically, a step in the method of processing an analysis card, according to the invention
- FIG. 2 shows this same analysis card, as obtained after the step or operation shown diagrammatically in Figure 1;
- - Figures 3 to 5 show respectively, still schematically, three successive steps of a treatment method according to the invention, implemented with an analysis card produced according to another embodiment of the invention;
- - Figure 6 shows, schematically, a device for processing an analysis card, according to the invention.
- the analysis card 1 shown is intended to cooperate with or adapted to a laser light source 4, emitting a coherent light or light beam 5, having a predetermined wavelength ⁇ , and a predetermined light power P.
- the analysis card 1 has a substantially flattened general shape, and comprises, in an assembled manner, for example by gluing, a flat body 14, for example a polystyrene or polycarbonate wafer, previously engraved or imprinted, as described below, between two external walls, or films 15 and 16, for example of transparent plastic vis-à-vis the light beam.
- the films 15 and 16 can be made of polypropylene, silicon or germanium.
- two chambers 2 and 3 are obtained and included within the analysis card 1, being, on the one hand each isolated from the outside of the card, and on the other hand isolated initially one relative to the other.
- the two chambers 2 and 3 are separated from each other by a partition 7 which can be pierced by the laser light from the source 4, made of absorbent material, in particular plastic, absorbing light energy of length d wave ⁇ of the laser source, in order to transform it into thermal or calorific energy capable of eliminating or making disappear at least locally or punctually the material of the partition 7.
- Two cavities 8 and 9 are formed on either side of the partition 7, and are respectively in communication with the two chambers 2 and 3.
- the arrangements described above are obtained in the following manner: - in the body 14, the two chambers 2 and 3 are imprinted or engraved, as well as the two cavities 8 and 9; and the external walls 15 and 16 close these chambers and cavities with respect to the outside;
- the chamber 2 is located below the cavity 8, and the chamber 3 is located above the cavity 9; one 2 of the chambers and the cavity 8 which corresponds to it are closed by one of the external walls, and the other chamber 3 and the other cavity 9 which corresponds to it, are closed by the other external wall 16;
- the perforable partition 7 is formed in the flat body 14, and therefore in its constituent material which is absorbing light energy of wavelength ⁇ ; -
- the two windows 10 and 11 are formed in the external walls 15 and 16 respectively, of which the constituent material is, as said above, transparent for the wavelength ⁇ .
- the processing method according to the invention comprises the following steps:
- the analysis card 1 has the structure and arrangement described above, characterized mainly by the partition 7, disposed within the card 1, capable of receiving light from the source 4, through window 10, in the form of an incident light ray 12; (c) the analysis card 1 is placed with respect to the light beam 5, so that the incidence of the light ray 12 illuminating the partition 7 is substantially perpendicular to the latter; (d) the laser light source 4 is controlled or controlled, so that the thermal energy dissipated within the partition 7 does not exceed that necessary for the local elimination or disappearance of the absorbent material constituting the partition 7, according to a hole 7a (see Figure 2) perforating the partition 7, of limited radial extension, that is to say just sufficient to establish communication or full passage between the cavities 8 and 9, and therefore between the chambers 2 and 3.
- the incidence of the light ray 12 illuminating the partition 7 is at the same time substantially perpendicular to the plane of the analysis card 1, and corresponds to the reference direction 6 of the light beam 5 emitted by the source 4.
- the axis of the light ray 12 illuminating the partition 7 crosses the latter substantially at its center, providing an edge on either side of the perforating hole 7a, not affected by the light energy of the laser beam.
- the light ray 12 illuminating the partition 7 is convergent according to a focal point 13 disposed in the center or within the partition 7.
- the light ray 12 can also be, or parallel, or divergent, for the purposes of the illumination of the partition 7, according to the distribution of the light energy, desired in the impact zone of the light ray 12.
- the movement of the liquid present in the chamber 3 is controlled, for example by capillarity and / or suction, so that the cavity 9, on the other side of the cavity 8 incidence relative to the perforable partition 7, remains full or empty of any liquid.
- a cavity 9 remaining empty of any liquid at the time of illumination with the light beam 5 makes it possible in particular to preserve the liquid or the liquids circulating in the analysis card, from any untimely or excessive heating.
- FIG. 3 to 5 differs from that shown in Figures 1 to 2, in that the analysis card 1 comprises "n", in this case 3 chambers 2, 3, 17, arranged in series , but can also be arranged in parallel, separated two by two by "n-1", in this case two perforable partitions 7 and 18, "n” being an integer, and one of the chambers 2,3 and 17 possibly including an optical measurement chamber.
- the analysis card 1 comprises "n", in this case 3 chambers 2, 3, 17, arranged in series , but can also be arranged in parallel, separated two by two by "n-1", in this case two perforable partitions 7 and 18, "n” being an integer, and one of the chambers 2,3 and 17 possibly including an optical measurement chamber.
- the perforable partitions 7 and 18 are distributed in the card 1, so that two partitions cannot be aligned with a single incident light beam 12
- the analysis card of Figures 3 to 5 includes a liquid filling the chamber 3, which will flow towards the chamber 2, after perforation of the partition 7, as shown in Figure 4, then towards the chamber 17 , after perforation of the partition 18, as partially shown in Figure 5.
- a device 19 for processing an analysis card 1 comprises: - a generator 20 of coherent light, having the predetermined wavelength ⁇ and the light power P, comprising a laser source, and means 25 for collimating and shaping the light beam emitted by the laser source; a beam of limited power, for example 2 mW, is emitted by a pointer in visible light and superimposed on the laser beam for its guidance;
- Optical means 29 for coupling the quasi-parallel light beam, to inject the latter into an optical fiber 21, or optical guide means such as a prism or lens, with good efficiency;
- - optical means 30 for collimating and / or shaping the beam, making it possible to obtain a circular "spot" of diameter and power density, determined on the work surface where the drilling will be carried out, located on or in each partition 7 or 18;
- the generator 20 emits light at 800 nm, with guide light at 670 nm.
- the power of the light source thus constituted is
- the optical fiber 21 used is a multimode fiber with a core diameter of 200 ⁇ m.
- a lens 30 makes it possible to focus the light energy on the center 13, located on or in each partition 7 or 18.
- - partition 7 or 18 made of polystyrene, having a thickness of 0.3 mm;
- the present invention can be implemented according to different embodiments; in particular one of the chambers, placed in communication according to the present invention, can itself communicate with the atmosphere or the environment in which the analysis card is located.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Credit Cards Or The Like (AREA)
- Sampling And Sample Adjustment (AREA)
- Multi-Process Working Machines And Systems (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Investigating Or Analyzing Materials Using Thermal Means (AREA)
- Optical Measuring Cells (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9601984 | 1996-02-12 | ||
FR9601984A FR2744803B1 (fr) | 1996-02-12 | 1996-02-12 | Procede et dispositif de traitement d'une carte d'analyse |
PCT/IB1997/000112 WO1997028899A1 (fr) | 1996-02-12 | 1997-02-12 | Carte d'analyse |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0820348A1 true EP0820348A1 (de) | 1998-01-28 |
EP0820348B1 EP0820348B1 (de) | 2002-01-09 |
Family
ID=9489316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97901736A Expired - Lifetime EP0820348B1 (de) | 1996-02-12 | 1997-02-12 | Testkarte für analysen |
Country Status (7)
Country | Link |
---|---|
US (1) | US5869002A (de) |
EP (1) | EP0820348B1 (de) |
AT (1) | ATE211657T1 (de) |
CA (1) | CA2218415C (de) |
DE (1) | DE69709499T2 (de) |
FR (1) | FR2744803B1 (de) |
WO (1) | WO1997028899A1 (de) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19716683C1 (de) * | 1997-04-21 | 1998-06-04 | Fraunhofer Ges Forschung | Vorrichtung zur getrennten, gekapselten Aufnahme einer Mehrzahl gleicher oder unterschiedlicher Stoffe |
DE19858443A1 (de) * | 1998-12-17 | 2000-07-06 | Inst Mikrotechnik Mainz Gmbh | Verfahren zum Abgeben eines Fluids, fluidisches Bauteil sowie Vorrichtung zur Handhabung solcher Bauteile |
WO2002000347A2 (en) * | 2000-06-28 | 2002-01-03 | 3M Innovative Properties Company | Sample processing devices, systems and methods |
US6720187B2 (en) * | 2000-06-28 | 2004-04-13 | 3M Innovative Properties Company | Multi-format sample processing devices |
US6734401B2 (en) | 2000-06-28 | 2004-05-11 | 3M Innovative Properties Company | Enhanced sample processing devices, systems and methods |
US7347976B2 (en) * | 2001-12-20 | 2008-03-25 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using a hydrophilic solid support in a hydrophobic matrix |
US7192560B2 (en) * | 2001-12-20 | 2007-03-20 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using anion exchange |
US6889468B2 (en) * | 2001-12-28 | 2005-05-10 | 3M Innovative Properties Company | Modular systems and methods for using sample processing devices |
DE10200541A1 (de) * | 2002-01-09 | 2003-07-24 | Zeiss Carl Jena Gmbh | Mikrotiterplatte |
WO2004050244A1 (en) * | 2002-11-29 | 2004-06-17 | The National Blood Authority | Opening sample containers using laser |
US7152616B2 (en) * | 2002-12-04 | 2006-12-26 | Spinx, Inc. | Devices and methods for programmable microscale manipulation of fluids |
EP1930635A3 (de) * | 2002-12-04 | 2008-08-13 | Spinx, Inc. | Vorrichtungen und Verfahren zur programmierbaren Mikrohandhabung von Fluiden |
US7981600B2 (en) * | 2003-04-17 | 2011-07-19 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using an anion exchange material that includes a polyoxyalkylene |
US20050130177A1 (en) | 2003-12-12 | 2005-06-16 | 3M Innovative Properties Company | Variable valve apparatus and methods |
US7939249B2 (en) * | 2003-12-24 | 2011-05-10 | 3M Innovative Properties Company | Methods for nucleic acid isolation and kits using a microfluidic device and concentration step |
US20070095393A1 (en) * | 2004-03-30 | 2007-05-03 | Piero Zucchelli | Devices and methods for programmable microscale manipulation of fluids |
JP4516346B2 (ja) * | 2004-04-14 | 2010-08-04 | 積水化学工業株式会社 | マイクロ全分析システム |
EP1693471A1 (de) * | 2005-02-16 | 2006-08-23 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Verfahren zum Raffinieren von Kohlenhydratenlösung enthaltender Flussigkeit |
EP1899064A2 (de) * | 2005-06-03 | 2008-03-19 | Spinx, Inc. | Dosimeter zur programmierbaren manipulation von fluiden auf mikromassstab |
US7763210B2 (en) * | 2005-07-05 | 2010-07-27 | 3M Innovative Properties Company | Compliant microfluidic sample processing disks |
US7323660B2 (en) * | 2005-07-05 | 2008-01-29 | 3M Innovative Properties Company | Modular sample processing apparatus kits and modules |
US7754474B2 (en) | 2005-07-05 | 2010-07-13 | 3M Innovative Properties Company | Sample processing device compression systems and methods |
US20070031282A1 (en) * | 2005-08-04 | 2007-02-08 | Piero Zucchelli | Devices and methods for interfacing microfluidic devices with fluid handling devices |
US8464760B2 (en) * | 2006-08-16 | 2013-06-18 | Samsung Electronic Co., Ltd. | Valve unit, reaction apparatus with the same, and method of forming valve in channel |
CN101568385B (zh) | 2006-12-22 | 2012-08-15 | 3M创新有限公司 | 用于微流体系统的热转移方法和结构 |
CN101568384B (zh) * | 2006-12-22 | 2013-05-01 | 3M创新有限公司 | 改进的样品处理装置、系统和方法 |
EP2140001A2 (de) * | 2007-04-25 | 2010-01-06 | 3M Innovative Properties Company | Verfahren zur amplifikation von nukleinsäuren |
WO2010084190A1 (en) * | 2009-01-23 | 2010-07-29 | Dublin City University | Fluidic single use valve and microfluidic systems incorporating said valve |
USD638951S1 (en) | 2009-11-13 | 2011-05-31 | 3M Innovative Properties Company | Sample processing disk cover |
US8834792B2 (en) | 2009-11-13 | 2014-09-16 | 3M Innovative Properties Company | Systems for processing sample processing devices |
USD638550S1 (en) | 2009-11-13 | 2011-05-24 | 3M Innovative Properties Company | Sample processing disk cover |
US20110117607A1 (en) * | 2009-11-13 | 2011-05-19 | 3M Innovative Properties Company | Annular compression systems and methods for sample processing devices |
USD667561S1 (en) | 2009-11-13 | 2012-09-18 | 3M Innovative Properties Company | Sample processing disk cover |
USD672467S1 (en) | 2011-05-18 | 2012-12-11 | 3M Innovative Properties Company | Rotatable sample processing disk |
CN103501908B (zh) | 2011-05-18 | 2016-03-16 | 3M创新有限公司 | 用于样品处理装置上阀调的系统和方法 |
EP2709762B1 (de) | 2011-05-18 | 2021-03-31 | DiaSorin S.p.A. | Vorrichtung und verfahren zum erkennen eines vorbestimmten volumens eines materials in einer probenverarbeitungsvorrichtung |
ES2755078T3 (es) | 2011-05-18 | 2020-04-21 | Diasorin S P A | Sistemas y métodos para medición volumétrica en un dispositivo de procesamiento de muestra |
CN103394382A (zh) * | 2013-08-07 | 2013-11-20 | 苏州扬清芯片科技有限公司 | 一种具有滤光特性的微流控芯片 |
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US5362654A (en) * | 1984-07-20 | 1994-11-08 | Sangstat Medical Corporation | Self-contained quantitative assay |
EP0244394B1 (de) * | 1986-04-23 | 1992-06-17 | AVL Medical Instruments AG | Sensorelement zur Bestimmung von Stoffkonzentrationen |
US5137808A (en) * | 1987-04-07 | 1992-08-11 | Syntex (U.S.A.) Inc. | Immunoassay device |
US5472671A (en) * | 1989-04-26 | 1995-12-05 | Nilsson; Sven-Erik | Cuvette |
US5364591A (en) * | 1992-06-01 | 1994-11-15 | Eastman Kodak Company | Device for moving a target-bearing solid through a liquid for detection while being contained |
US5290518A (en) * | 1992-08-17 | 1994-03-01 | Eastman Kodak Company | Flexible extraction device with burstable sidewall |
JP3594979B2 (ja) * | 1992-10-23 | 2004-12-02 | イーストマン コダック カンパニー | 核酸材料の増大及び検出用収納装置 |
US5500187A (en) * | 1992-12-08 | 1996-03-19 | Westinghouse Electric Corporation | Disposable optical agglutination assay device and method for use |
US5411065A (en) * | 1994-01-10 | 1995-05-02 | Kvm Technologies, Inc. | Liquid specimen transfer apparatus and method |
-
1996
- 1996-02-12 FR FR9601984A patent/FR2744803B1/fr not_active Expired - Fee Related
-
1997
- 1997-02-12 US US08/913,726 patent/US5869002A/en not_active Expired - Lifetime
- 1997-02-12 AT AT97901736T patent/ATE211657T1/de not_active IP Right Cessation
- 1997-02-12 WO PCT/IB1997/000112 patent/WO1997028899A1/fr active IP Right Grant
- 1997-02-12 EP EP97901736A patent/EP0820348B1/de not_active Expired - Lifetime
- 1997-02-12 DE DE69709499T patent/DE69709499T2/de not_active Expired - Lifetime
- 1997-02-12 CA CA002218415A patent/CA2218415C/fr not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
See references of WO9728899A1 * |
Also Published As
Publication number | Publication date |
---|---|
CA2218415C (fr) | 2006-05-30 |
US5869002A (en) | 1999-02-09 |
FR2744803B1 (fr) | 1998-03-13 |
DE69709499T2 (de) | 2002-09-26 |
ATE211657T1 (de) | 2002-01-15 |
EP0820348B1 (de) | 2002-01-09 |
WO1997028899A1 (fr) | 1997-08-14 |
FR2744803A1 (fr) | 1997-08-14 |
CA2218415A1 (fr) | 1997-08-14 |
DE69709499D1 (de) | 2002-02-14 |
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